Issue 49, 2017, Issue in Progress

Rhodium(iii)-catalyzed indole-directed carbenoid aryl C–H insertion/cyclization: access to 1,2-benzocarbazoles

Abstract

A rhodium(III)-catalyzed indole-directed aryl C–H bond carbenoid insertion cascade of 2-arylindoles with diazo compounds has been developed. This method provides a rapid access to 1,2-benzocarbazoles and isoquinoline-based polycyclic heteroaromatics with a broad range of functional group tolerance. The primary evaluation of the photoluminescence property of the novel extended π-systems indicated that these heteroarenes could be potentially used in the field of optoelectronic materials.

Graphical abstract: Rhodium(iii)-catalyzed indole-directed carbenoid aryl C–H insertion/cyclization: access to 1,2-benzocarbazoles

Supplementary files

Article information

Article type
Paper
Submitted
01 May 2017
Accepted
08 Jun 2017
First published
13 Jun 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 30554-30558

Rhodium(III)-catalyzed indole-directed carbenoid aryl C–H insertion/cyclization: access to 1,2-benzocarbazoles

Z. Zhang, K. Liu, X. Chen, S. Su, Y. Deng and W. Zeng, RSC Adv., 2017, 7, 30554 DOI: 10.1039/C7RA04889K

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